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甲氧苄啶-磺胺甲恶唑对产KPC革兰氏阴性病原体所致感染的体外抗菌活性及临床应用:综述

In vitro antimicrobial activity and clinical use of trimethoprim-sulfamethoxazole for infections due to KPC-producing Gram-negative pathogens: a review.

作者信息

Falagas Matthew E, Kontogiannis Dimitrios S, Sargianou Maria, Kakoullis Stylianos A

机构信息

Alfa Institute of Biomedical Sciences (AIBS), 9 Neapoleos Street, 151 23 Marousi, Athens, Greece.

European University Cyprus School of Medicine, Nicosia, Cyprus.

出版信息

Eur J Clin Microbiol Infect Dis. 2025 Aug 14. doi: 10.1007/s10096-025-05236-z.

Abstract

KPC-producing Gram-negative pathogens have disseminated worldwide and cause infections of various organs and systems. Given the limited therapeutic options for such infections, trimethoprim-sulfamethoxazole may be a consideration. We evaluated the available in vitro and clinical data on trimethoprim-sulfamethoxazole for treating patients with infections caused by KPC-producing pathogens. Five resources (Embase, Google Scholar, Scopus, PubMed, and Web of Science) were used for identifying relevant studies. In total, 12 in vitro studies were included. These studies demonstrated that the susceptibility of KPC-producing pathogens to trimethoprim-sulfamethoxazole ranged from 7 to 100% (> 70% in 7/12 studies), and the minimum inhibitory concentration (MIC) ranged from ≤ 0.25 (in 2 studies) to > 32 (in 2 studies) mg/L. Additionally, a prospective cohort study evaluated 14 patients who received trimethoprim-sulfamethoxazole to treat infections caused by KPC-producing bacteria. Of those, 13 out of 14 (93%) patients achieved a clinical cure. Clinical published data assessing trimethoprim-sulfamethoxazole's effectiveness for treating infections due to KPC-producing Gram-negative pathogens are limited. While data from in vitro studies suggest the consideration of trimethoprim-sulfamethoxazole when pathogens are susceptible, more clinical evidence is needed to use the drug safely in this population.

摘要

产KPC的革兰氏阴性病原体已在全球传播,并导致各种器官和系统感染。鉴于此类感染的治疗选择有限,复方磺胺甲恶唑可能是一种选择。我们评估了关于复方磺胺甲恶唑治疗产KPC病原体感染患者的现有体外和临床数据。使用了五个资源库(Embase、谷歌学术、Scopus、PubMed和科学网)来识别相关研究。总共纳入了12项体外研究。这些研究表明,产KPC病原体对复方磺胺甲恶唑的敏感性范围为7%至100%(12项研究中有7项>70%),最低抑菌浓度(MIC)范围为≤0.25(2项研究)至>32(2项研究)mg/L。此外,一项前瞻性队列研究评估了14例接受复方磺胺甲恶唑治疗产KPC细菌感染的患者。其中,14例患者中有13例(93%)临床治愈。评估复方磺胺甲恶唑治疗产KPC革兰氏阴性病原体感染有效性的临床发表数据有限。虽然体外研究数据表明,当病原体敏感时可考虑使用复方磺胺甲恶唑,但需要更多临床证据才能在此类人群中安全使用该药物。

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